新合成的具有哒嗪桥接配体的双核铂(II)配合物的特性、与 DNA/BSA 生物大分子的相互作用模式及抗肿瘤活性

IF 2.7 3区 化学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY JBIC Journal of Biological Inorganic Chemistry Pub Date : 2023-12-15 DOI:10.1007/s00775-023-02030-0
Sanja Zornić, Bojana Simović Marković, Andjela A. Franich, Goran V. Janjić, Milka B. Jadranin, Jelena Avdalović, Snežana Rajković, Marija D. Živković, Nebojša N. Arsenijević, Gordana D. Radosavljević, Jelena Pantić
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引用次数: 0

摘要

铂类药物是公认的高效抗肿瘤药物,但也面临着多种不良反应。在此,我们设计了四种双核铂(II)配合物:[{Pt(1,2-pn)Cl}2(μ-pydz)]Cl2(C1)、[{Pt(ibn)Cl}2(μ-pydz)]Cl2(C2)、[{Pt(1,3-pn)Cl}2(μ-pydz)]Cl2(C3)和[{Pt(1,3-pnd)Cl}2(μ-pydz)]Cl2(C4)、pydz 是哒嗪,1,2-pn 是 ( ±)-1,2-丙二胺,ibn 是 1,2-二氨基-2-甲基丙烷,1,3-pn 是 1,3-丙二胺,1,3-pnd 是 1,3-戊二胺)。C1-C4 复合物与小牛胸腺 DNA(CT-DNA)的相互作用和结合能力已通过粘度测量、紫外可见光谱、荧光发射光谱和分子对接进行了监测。通过荧光发射光谱监测了 C1-C4 复合物与牛血清白蛋白(BSA)的结合亲和力。测试的复合物对不同的小鼠和人类肿瘤细胞系具有不同的细胞毒性。C2 的细胞毒性最强,尤其是对小鼠(4T1)和人类(MDA-MD468)乳腺癌细胞的毒性,其毒性呈剂量和时间依赖性。C2 可诱导 4T1 和 MDA-MD468 细胞凋亡,细胞周期亚 G1 期的细胞积累以及 4T1 细胞中执行 Caspase 3 和 Caspase 9 水平的升高进一步证明了这一点。C2 通过降低细胞周期蛋白 D3 和细胞周期蛋白 E 的表达以及提高抑制剂 p27 的水平,表现出抗增殖作用。此外,C2 还能下调参与控制肿瘤细胞增殖和死亡的癌基因 c-Myc 和磷酸化 AKT。为了测量细胞吸收铂(II)复合物的数量,对细胞中的铂含量进行了量化。然而,C2 未能抑制小鼠乳腺癌在体内的生长。图解摘要核铂(II)复合物[{Pt(ibn)Cl}2(μ-pydz)]Cl2在体外具有抗肿瘤活性,可诱导小鼠乳腺癌细胞凋亡并减少其增殖。然而,它对体内肿瘤生长的抑制作用却不明显。
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Characterization, modes of interactions with DNA/BSA biomolecules and anti-tumor activity of newly synthesized dinuclear platinum(II) complexes with pyridazine bridging ligand

Platinum-based drugs are widely recognized efficient anti-tumor agents, but faced with multiple undesirable effects. Here, four dinuclear platinum(II) complexes, [{Pt(1,2-pn)Cl}2(μ-pydz)]Cl2 (C1), [{Pt(ibn)Cl}2(μ-pydz)]Cl2 (C2), [{Pt(1,3-pn)Cl}2(μ-pydz)]Cl2 (C3) and [{Pt(1,3-pnd)Cl}2(μ-pydz)]Cl2 (C4), were designed (pydz is pyridazine, 1,2-pn is ( ±)-1,2-propylenediamine, ibn is 1,2-diamino-2-methylpropane, 1,3-pn is 1,3-propylenediamine, and 1,3-pnd is 1,3-pentanediamine). Interactions and binding ability of C1C4 complexes with calf thymus DNA (CT-DNA) has been monitored by viscosity measurements, UV–Vis, fluorescence emission spectroscopy and molecular docking. Binding affinities of C1C4 complexes to the bovine serum albumin (BSA) has been monitored by fluorescence emission spectroscopy. The tested complexes exhibit variable cytotoxicity toward different mouse and human tumor cell lines. C2 shows the most potent cytotoxicity, especially against mouse (4T1) and human (MDA-MD468) breast cancer cells in the dose- and time-dependent manner. C2 induces 4T1 and MDA-MD468 cells apoptosis, further documented by the accumulation of cells at sub-G1 phase of cell cycle and increase of executive caspase 3 and caspase 9 levels in 4T1 cells. C2 exhibits anti-proliferative effect through the reduction of cyclin D3 and cyclin E expression and elevation of inhibitor p27 level. Also, C2 downregulates c-Myc and phosphorylated AKT, oncogenes involved in the control of tumor cell proliferation and death. In order to measure the amount of platinum(II) complexes taken up by the cells, the cellular platinum content were quantified. However, C2 failed to inhibit mouse breast cancer growth in vivo. Chemical modifications of tested platinum(II) complexes might be a valuable approach for the improvement of their anti-tumor activity, especially effects in vivo.

Graphical abstract

Dinuclear platinum(II) complex [{Pt(ibn)Cl}2(μ-pydz)]Cl2 shows anti-tumor activity, triggers the apoptosis and reduces the proliferation of mouse breast cancer cells in vitro. However, its inhibitory effect on tumor growth in vivo is absent.

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来源期刊
JBIC Journal of Biological Inorganic Chemistry
JBIC Journal of Biological Inorganic Chemistry 化学-生化与分子生物学
CiteScore
5.90
自引率
3.30%
发文量
49
审稿时长
3 months
期刊介绍: Biological inorganic chemistry is a growing field of science that embraces the principles of biology and inorganic chemistry and impacts other fields ranging from medicine to the environment. JBIC (Journal of Biological Inorganic Chemistry) seeks to promote this field internationally. The Journal is primarily concerned with advances in understanding the role of metal ions within a biological matrix—be it a protein, DNA/RNA, or a cell, as well as appropriate model studies. Manuscripts describing high-quality original research on the above topics in English are invited for submission to this Journal. The Journal publishes original articles, minireviews, and commentaries on debated issues.
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